Canonical Allele Identifier: PA106396
Gene: PDGFRB HGNC NCBI

Linked Data

ClinVar Variation Id: 55848
ClinVar RCV Id: RCV000049264 RCV000390507 RCV000454370 RCV001197225 RCV001201357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002600.1:p.Arg561Cys
CA328075
NM_002609.3:c.1681C>T